2019-10-30

IBD, the NHS and me – my story of how I need to second guess if I need medical help

I found this post in my drafts folder, I am not sure why I did not post it at the time. This is an account of what happened in January 2018 and why it is important to not second guess yourself if you need medical attention. I am publishing it now as I am working
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Falling apart in word tiles

Things I need to cope with chronic illness

Five years ago I was diagnosed with my first chronic illness. Fibromyalgia. Two years later I had various tests as I believed that my body was telling me that something more was happening underneath. I was told that it was all just down to fibro, and from then on, everything was down to fibro. Fast
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Fed up in a hospital bed

Living with Crohns Disease

Quite simply, it’s shit.  Yes, I am talking about both the illness and the fact that having crohns is a pain in the… neck! If you do not know already from following my hospital and toast updates via social media, since the end of July I have been rather poorly. To date, there have been
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